7 results
·
30ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
MOTOCLIP SUPER ELASTIC FUSION SYSTEM
FDA Adverse Event
Injury
·CROSSROADS EXTREMITY SYSTEMS LLC·Product code JDR·May 10, 2019
ACCU-CHEK ® SPIRIT
FDA Adverse Event
Injury
·ROCHE HEALTH SOLUTIONS INC·Product code LZG·March 19, 2013
MINI-CAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·March 9, 2011
9600+
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·March 11, 2008
BD VACUTAINER® BUFFERED SODIUM CITRATE (9NC) BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·September 12, 2018
BD¿ VACUTAINER® BUFFERED SODIUM CITRATE BLOOD COLLECTION TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·November 21, 2018
MEDTRONIC TRANSCATHETER VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·August 24, 2022